PMID: 24175826

Li XF, He HB, Zhu YS, He JK, Ye WW, Chen YX, Lou LQ
Association between the c.3751G>a genetic variant of MDR1 and hepatocellular carcinoma risk in a Chinese Han population.
Asian Pac J Cancer Prev. 2013;14(9):5361-5., [PubMed]
Sentences
No. Mutations Sentence Comment
49 ABCB1 p.Val1251Ile
X
ABCB1 p.Val1251Ile 24175826:49:240
status: NEW
view ABCB1 p.Val1251Ile details
 Based on the results of DNA sequence analysis, the c.3751G>Agenetic variant is a non-synonymous mutation, which caused by G toAmutations in exon29 of human MDR1 gene and led to the valine (Val) to isoleucine (Ile) amino acid replacement (p.Val1251Ile, Reference sequences GenBank IDs: NG_011513.1, NM_000927.4 and NP_000918.2). Login to comment 74 ABCB1 p.Val1251Ile
X
ABCB1 p.Val1251Ile 24175826:74:72
status: NEW
view ABCB1 p.Val1251Ile details
 Sequence analyses indicate that this genetic variant results into the p.Val1251Ile amino acid replacement. Login to comment